1997
DOI: 10.1016/s0344-0338(97)80016-7
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Hashimoto's Thyroiditis Associated with Riedel's Thyroiditis and Retroperitoneal Fibrosis

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Cited by 24 publications
(15 citation statements)
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“…Hashimoto thyroiditis has also been reported to be associated with IgG4-related retroperitoneal fibrosis, 29,30 and might be classified into IgG4-positive and -negative thyroid lesions on the basis of immunohistochemistry. 31,32 Thus, the 4 patients could be diagnosed with IgG4-related disease with the involvement of bilateral or unilateral lacrimal gland.…”
Section: Discussionmentioning
confidence: 99%
“…Hashimoto thyroiditis has also been reported to be associated with IgG4-related retroperitoneal fibrosis, 29,30 and might be classified into IgG4-positive and -negative thyroid lesions on the basis of immunohistochemistry. 31,32 Thus, the 4 patients could be diagnosed with IgG4-related disease with the involvement of bilateral or unilateral lacrimal gland.…”
Section: Discussionmentioning
confidence: 99%
“…A number of cases with features consistent with both diseases have been described [12], inferring that the sequence of events in Riedel’s thyroiditis might have initiated as Hashimoto’s thyroiditis [10]. Our patient has a number of features consistent with a diagnosis of both Hashimoto’s and Riedel’s thyroiditis.…”
Section: Discussionmentioning
confidence: 54%
“…Previous reports associate Riedel’s thyroiditis with multifocal systemic fibrosclerosis [2] which may include sclerosing cholangitis [6], fibrosing mediastinitis [7] apical lung fibrosis [8,9], and retroperitoneal fibrosis [10,11,12]. Although fibrotic lung nodules have not been previously described in Riedel’s thyroiditis, a similar appearance has been reported in IgG4-associated multifocal systemic fibrosclerosis [13], which can include Riedel’s thyroiditis.…”
Section: Discussionmentioning
confidence: 84%
“…While both RT and IgG4-RD have been reported to occur more frequently in patients with hypothyroidism and those who are highly positive for anti-thyroid antibodies, RT is more common in women between 30 and 50 years of age [8,7,[24][25][26], and IgG4-RD has a higher incidence in men older than 50 years [17,27]. Our 10 Japanese patients with RT were predominantly females (70%), aged 30 to 60 years, which was rather consistent with the clinical profile of RT.…”
Section: Methodsmentioning
confidence: 99%